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1234819007: Limb girdle muscular dystrophy due to protein O-mannose kinase deficiency (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5084104014 Limb girdle muscular dystrophy due to protein O-mannose kinase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5084105010 Limb girdle muscular dystrophy due to POMK deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5084106011 Limb girdle muscular dystrophy due to protein O-mannose kinase deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5084107019 A form of limb-girdle muscular dystrophy presenting in infancy with muscle weakness and delayed motor development (eventually learning to walk at 18 months of age) followed by progressive proximal weakness, pseudohypertrophy of calf muscles, mild facial weakness and borderline intelligence. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
13732021000172115 'limb-girdle'-spierdystrofie door POMK-deficiëntie nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
13732031000172117 LGMD door POMK-deficiëntie nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)
13732041000172112 'limb-girdle'-spierdystrofie door deficiëntie van 'protein O-mannose kinase' nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
13732051000172114 gordeldystrofie door POMK-deficiëntie nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Limb girdle muscular dystrophy due to POMK deficiency Is a Inherited metabolic disorder of nervous system true Inferred relationship Some
Limb girdle muscular dystrophy due to POMK deficiency Is a Chronic nervous system disorder (disorder) true Inferred relationship Some
Limb girdle muscular dystrophy due to POMK deficiency Is a Chronic metabolic disorder true Inferred relationship Some
Limb girdle muscular dystrophy due to POMK deficiency Is a Carbohydrate-deficient glycoprotein syndrome true Inferred relationship Some
Limb girdle muscular dystrophy due to POMK deficiency Is a Autosomal recessive muscular dystrophy with limb girdle distribution true Inferred relationship Some
Limb girdle muscular dystrophy due to POMK deficiency Clinical course Progressive (qualifier value) true Inferred relationship Some 3
Limb girdle muscular dystrophy due to POMK deficiency Occurrence Congenital true Inferred relationship Some 2
Limb girdle muscular dystrophy due to POMK deficiency Finding site Structure of nervous system (body structure) true Inferred relationship Some 4
Limb girdle muscular dystrophy due to POMK deficiency Finding site Skeletal muscle structure (body structure) true Inferred relationship Some 1
Limb girdle muscular dystrophy due to POMK deficiency Associated morphology Dystrophy true Inferred relationship Some 1
Limb girdle muscular dystrophy due to POMK deficiency Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Limb girdle muscular dystrophy due to POMK deficiency Is a Developmental delay true Inferred relationship Some
Limb girdle muscular dystrophy due to POMK deficiency Occurrence Infancy true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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